ClinVar Miner

Submissions for variant NM_000130.5(F5):c.251-6del

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003409235 SCV004126283 likely benign not provided 2023-10-01 criteria provided, single submitter clinical testing F5: BP4
Labcorp Genetics (formerly Invitae), Labcorp RCV003596248 SCV004310356 benign Congenital factor V deficiency 2024-11-19 criteria provided, single submitter clinical testing

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